Canonical Allele Identifier: CA11429796

Gene: MCCC1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.183020499G>A , CM000665.2:g.183020499G>A	GRCh38
NC_000003.11:g.182738287G>A , CM000665.1:g.182738287G>A	GRCh37
NC_000003.10:g.184220981G>A	NCBI36
NG_008100.1:g.84079C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_020166.5:c.1870-262C>T MANE Select	NP_064551.3:n.1870-262C>T
ENST00000265594.9:c.1870-262C>T MANE Select	ENSP00000265594.4:n.1870-262C>T
NM_001293273.1:c.1519-262C>T	NP_001280202.1:n.1519-262C>T
NM_001293273.2:c.1519-262C>T	NP_001280202.1:n.1519-262C>T
NM_001363880.1:c.1543-262C>T	NP_001350809.1:n.1543-262C>T
NM_020166.4:c.1870-262C>T	NP_064551.3:n.1870-262C>T
NR_120639.1:n.1734-262C>T
NR_120639.2:n.1643-262C>T
NR_120640.1:n.2417-262C>T
NR_120640.2:n.2417-262C>T
ENST00000265594.8:c.1870-262C>T	ENSP00000265594.4:n.1870-262C>T
ENST00000464601.5:n.302-262C>T
ENST00000476176.5:c.1729-262C>T	ENSP00000420433.1:n.1729-262C>T
ENST00000492597.5:c.1543-262C>T	ENSP00000419898.1:n.1543-262C>T
ENST00000495767.5:c.*1401-262C>T	ENSP00000419658.1:n.*1401-262C>T
ENST00000497830.5:c.*1467-262C>T	ENSP00000420088.1:n.*1467-262C>T
ENST00000497959.5:c.*331-262C>T	ENSP00000420648.1:n.*331-262C>T
ENST00000539926.5:c.1420-262C>T	ENSP00000441253.2:n.1420-262C>T
ENST00000610757.4:c.1420-262C>T	ENSP00000480435.1:n.1420-262C>T
ENST00000629669.2:c.*234-262C>T	ENSP00000486824.1:n.*234-262C>T
XM_006713702.1:c.1543-262C>T	XP_006713765.1:n.1543-262C>T
XM_011512992.1:c.1756-262C>T	XP_011511294.1:n.1756-262C>T
XM_011512992.2:c.1756-262C>T	XP_011511294.1:n.1756-262C>T
XR_001740207.2:n.2090-262C>T
XR_001740208.2:n.1943-262C>T
XR_001740209.2:n.1696-262C>T
XR_001740210.1:n.1773-262C>T
XR_241502.2:n.1800-262C>T
XR_241502.3:n.1746-262C>T